FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FIBERBRONCHOSCOPE (PENTAX FB-17A)

K Number: K760171 · Decision Jul 19, 1976
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
39
Review Days
13

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Basic Information

Device Name
FIBERBRONCHOSCOPE (PENTAX FB-17A)
K Number
K760171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Pilling Co.
Date Received
July 6, 1976
Decision Date
July 19, 1976
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

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K922971 NO-SCALPEL VASCETOMY INSTRUMENTS
K914015 CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP
K911099 MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE
K911100 MEHIGAN-PILLING PHLEBETOME TM
K904507 PILLING BRUSH VALVULOTOME
K884946 JEHLE CORONARY PERFUSION CATHETERS
K882930 LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX
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